Study to Determine the Pharmacokinetics, Safety & Tolerability of Aripiprazole in Adults With Schizophrenia

Completed · Phase 1

Conditions studied: Schizophrenia

In brief

This trial will determine the Pharmacokinetics, safety and tolerability of single-dose Aripiprazole administered intramuscularly in adults with schizophrenia

Key facts

Study ID

NCT03150771

Run by

Otsuka Pharmaceutical Development & Commercialization, Inc.

People needed

36

Starts

2017-06-14

Expected to finish

2018-05-02

Last updated by the study team

2018-06-12

Who can join

Age: 18 and older, up to 64. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male and female individuals between 18 and 64 years, inclusive, at screening with a current diagnosis of schizophrenia as defined by Diagnostic and Statistical Manual of Mental Disorders: edition 5 (DSM-5)
• Body mass index (BMI) between 18 and 35 kg/m\^2 at screening
• Male and female subjects who are surgically sterile, female subjects who have been postmenopausal for at least 12 consecutive months prior to screening or male/female subjects who agree to remain abstinent or practice 2 of the approved birth control methods from screening for at least 150 days after dose of Investigational Medical Product (IMP) for female subjects or 180 days after dose of IMP for male subjects.
• Documented history of previously tolerating Aripiprazole per investigator's judgment.

You may not qualify if…

• Met DSM-5 criteria for substance use disorder within past 180 days
• Positive drug screen for drugs of abuse
• Use of more than 1 antipsychotic medication at screening or baseline, except for oral Aripiprazole administered during tolerability testing and current antipsychotic medication
• Subjects may not receive varenicline beyond the screening visit.
• Subjects who had participated in any clinical trial involving a psychotropic medication within 1 month prior to administration of IMP
• Major surgery within 30 days prior to administration of IMP or surgery during the trial
• Subjects at significant risk of committing suicide based on history, psychiatric exams
• Subjects currently in an acute relapse of schizophrenia
• Subjects with a current DSM-5 diagnosis other than schizophrenia
• Subjects with a history of neuroleptic malignant syndrome, seizure disorder, or clinically significant tardive dyskinesia
• Subjects who have had electroconvulsive therapy within 2 months prior to administration of IMP
• Females who are breast-feeding and/or who have a positive pregnancy test result prior to receiving IMP
• History of or current hepatitis or Acquired Immunodeficiency Syndrome or carriers of Hepatitis B surface antigen (HBsAG), Hepatitis C antigen (anti-HCV) and/or Human Immunodeficiency Virus (HIV) antibodies

Where it is running

• Woodland International Research Group — Little Rock, Arkansas, United States
• CNRI-San Diego — San Diego, California, United States
• Community Clinical Research Inc. — Austin, Texas, United States

Full record on ClinicalTrials.gov

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